Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
62687962
Legacy Mutation ID ( COSN )
COSN26859342
FATHMM-MKL Score
0.0868 (not functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
62687962
Syntax
6:g.26376713T>C
Type
Substitution
Sample/Tissue
W1T / Thyroid
References
Studies
676
Genome Location
6:26376713..26376713
Browser Links